Scientific Affairs Lead

Published
May 14, 2022
Location
San Mateo, CA
Job Type

Description

IVD, RUO, Medical Device, Molecular Product Development

This Jobot Job is hosted by: Andrew Duong
Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume.
Salary: $100,000 - $140,000 per year

A bit about us:

We are a Series C startup with new assay development on the horizon and we are utilizing cutting-edge molecular and automation technology to make global impact to help combat diseases & pathogens through the power of genomics. We are a seeking humble and ambitious individuals to help us achieve our goals and make great impact at scale with our work

Why join us?

We are a startup with extensive investors and a leadership board comprised of industry best executives with a guide to success for market penetration, timing has met opportunity and we're in growth mode. We offer competitive pay, excellent benefits, flexibility, great office/lab amenities including catered food each week, and equity so you'll have a piece of the pie.

Job Details

Responsible for providing insight for clinical applications and user requirements for the product development process. Additionally, will provide medical and clinical insight to the business for existing product enhancements.
Build and manage scientific collateral and educational materials to facilitate the market adoption of company products.
Participates in relationships with customers, collaborators, government agents and professional associations as appropriate to keep informed of existing and evolving industry technologies and trends.
Provides consultation of company products to internal teams and local public health laboratories and builds professional contacts with Center for Disease Control and Prevention, regional public health laboratory networks and other stakeholders and customers
Participates and presents in professional associations and conferences e.g. ASM, APHL,
Review product labeling, marketing, advertising and promotional materials against internal policies and external guidance/regulations.
Conducts training and/or communicates appropriate materials, as needed, to enhance team’s knowledge of working in a regulated and public health laboratory environment.
Assists Quality/Regulatory department in the update, enhancement, and creation of internal policies and procedures.
Coordinate obtaining specimens from clients as needed for product development
Lead the scientific design of study protocols and reports for clinical trials e.g. designing databases and case reports as required
Present product information at different conferences for various audiences

Interested in hearing more? Easy Apply now by clicking the "Apply Now" button.

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